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Human Resistin Protein expressed in Escherichia coli (E. coli) - ABIN413761
Shen, Zhang, Gan, Wang, Wang, LeMaire, Coselli, Wang et al.: Up-regulation of PTEN (phosphatase and tensin homolog deleted on chromosome ten) mediates p38 MAPK stress signal-induced inhibition of insulin signaling. A cross-talk between stress signaling and ... in The Journal of biological chemistry 2006
Show all 2 Pubmed References
Human Resistin Protein expressed in HEK-293 Cells - ABIN2730725
Nakayama, Aoki, Uchihashi, Nishijima-Matsunobu, Yamamoto, Kakihara, Iwakiri, Fujimoto, Toda: Interaction between Esophageal Squamous Cell Carcinoma and Adipose Tissue in Vitro. in The American journal of pathology 2016
Mouse (Murine) Resistin Protein expressed in HEK-293 Cells - ABIN1344359
Daquinag, Zhang, Amaya-Manzanares, Simmons, Kolonin: An isoform of decorin is a resistin receptor on the surface of adipose progenitor cells. in Cell stem cell 2011
The effects of exogenous human kisspeptin-10 (KP10) were studied on three important adipokines, namely, adiponectin, leptin (show LEP Proteins), and resistin in a set of four chair-restraint habituated intact adult male rhesus monkeys.
Results demonstrate an association between RETN gene variants and risk of rheumatoid arthritis disease. RETN SNPs were significantly associated with clinical therapies and C-reactive protein serum marker of rheumatoid arthritis in the Chinese Han population.
Studied adiponectin (ADIPOQ), leptin (LEP (show LEP Proteins)), leptin receptor (LEPR (show LEPR Proteins)), and resistin (RETN) single nucleotide polymorphisms and their association in obesity. Results showed that ADIPOQ 4522CLEP (show LEP Proteins) 2548GRETN 420C
Results show that adiponectin, resistin and visfatin (show NAMPT Proteins) are present in osteophytes but have no direct influence on osteophyte development. Although these adipokines induce several inflammatory mediators, they do not affect osteoblast- or chondrocyte-related mechanisms of osteophyte development.
Fine-tuned by RETN SNPs, intrahepatic, multi-cellular resistin reinforced IFNL3 (show IL28B Proteins) in eliminating HCV via immunomodulation to counteract pro-inflammation.
Dementia of vascular origin is characterized by elevated resistin levels.
Resistin probably plays a role in the pathogenesis of hepatic insulin (show INS Proteins) resistance and aggravates pathologic changes in the liver of patients with non-alcoholic fatty liver disease
Resistin and NGAL (show LCN2 Proteins) correlate with expression of endothelial cell adhesion molecules in sepsis.
the role of resistin (an adipokine) in the development of gestational diabetes mellitus
high resistin levels are associated with increased obesity-related cancer risk [meta-analysis]
Results showed that the RETN SNP rs3219175 with AG or at least 1 A allele was associated with a higher risk of lung cancer than wild-type (GG) carriers. Moreover, the RETN SNP rs3219175 with AG or AG + AA alleles was associated with a higher risk of distant metastasis than that in patients carrying GG alleles.
Resistin-associated VSMC dysfunction and intimal hyperplasia are related to PKCepsilon (show PRKCE Proteins)-dependent Nox activation and ROS (show ROS1 Proteins) generation
Resistin may enhance inflammation by cross-talking with TLR4 (show TLR4 Proteins)/NF-kappaB (show NFKB1 Proteins) signaling during the development of coronary arteritis in mice
OLI (show TOMM22 Proteins) is a physiological repressor of systemic resistin release whereas FFA upregulate resistin release in vitro from adipocytes.
Resistin possibly acts via an intracrine pathway as an intracellular sensor, regulating the adipocyte insulin (show INS Proteins) sensitivity.
In 3T3-L1 adipocytes, catechin and quercetin attenuated TNF-alpha-induced elevated protein carbonyls, increased proinflammatory cytokine expression (MCP-1, resistin), and decreased adiponectin.
Mouse Resistin has regulative effects on murine bone marrow hematopoiesis.
murine resistin is increased in the lungs of wild-type mice following acute ozone exposure but does not promote ozone-induced lung pathology.
Inhibition of miR (show MLXIP Proteins)-696 restored the triglycerides content by up to 80%, which suggests that, in C2C12 cells, resistin at least partially increases the deposition of lipids through miR (show MLXIP Proteins)-696.
Resistin regulates PAI-1 (show SERPINE1 Proteins) expression in 3T3-L1 adipocytes via Akt (show AKT1 Proteins) phosphorylation.
Oxidized-LDL promotes the expression and secretion of visfatin (show NAMPT Proteins) and resistin through its activation of endoplasmic reticulum stress.
The data suggest that there is local cooperation between resistin and PPARgamma (show PPARG Proteins) expression in the porcine ovary. Resistin significantly increased the expression of PPARgamma (show PPARG Proteins), whereas PPARgamma (show PPARG Proteins) decreased resistin expression; thus, PPARgamma (show PPARG Proteins) is a new key regulator of resistin expression and function.
The expression, immunolocalization and concentration of resistin in different sized ovarian follicles, was investigated.
This gene belongs to the family defined by the mouse resistin-like genes. The characteristic feature of this family is the C-terminal stretch of 10 cys residues with identical spacing. The mouse homolog of this protein is secreted by adipocytes, and may be the hormone potentially linking obesity to type II diabetes. Alternatively spliced transcript variants encoding the same protein have been found for this gene.
, C/EBP-epsilon regulated myeloid-specific secreted cysteine-rich protein precursor 1
, adipose tissue-specific secretory factor
, c/EBP-epsilon-regulated myeloid-specific secreted cysteine-rich protein
, cysteine-rich secreted protein A12-alpha-like 2
, cysteine-rich secreted protein FIZZ3
, found in inflammatory zone 3
, resistin delta2
, adipose-specific cysteine-rich secreted protein A12-alpha
, dominant inhibitory adipocyte-specific secretory factor
, adipocyte specific secreted hormone